Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.22 (C)
Location

Chromosome 16:50769845 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ImmunoChip, Affy GenomeWideSNP_6.0

Variation displays